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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589675Generated: November 4, 2026

Benzyl 4-Hydroxybenzoate → 4-[(Benzyloxy)carbonyl]phenyl 4-(acetyloxy)benzoate

https://huagongshe.com/reaction/1589675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
ReactantTriethylamineHCID 8471—
Reactantp-Acetoxybenzoyl chlorideHCID 2756254—
SolventTolueneHCID 1140—
Product4-[(Benzyloxy)carbonyl]phenyl 4-(acetyloxy)benzoateHCID 13587739—

Reaction Conditions

Temperature30 °C

Reaction Steps

A 200 ml. four-necked flask equipped with a condenser tube and a thermometer was charged with 36 g of p-acetoxybenzoic acid and 71.4 g of thionyl chloride, and they were reacted at 50° C. for 4 hours. The excess of thionyl chloride was evaporated under reduced pressure to give p-acetoxybenzoyl chloride. Then, a 300 ml four-necked flask equipped with a condenser tube, a thermometer and a dropping funnel was charged with 45.7 g of benzyl p-hydroxybenzoate, 20.2 g of triethylamine and 100 ml of toluene. The temperature of the flask was raised to 30° C., and a solution of 39.7 g of p-acetoxybenzoyl chloride in 50 g of toluene was added dropwise over 1 hour, and the reaction was carried out at 50° C. for 30 minutes. After cooling, the reaction mixture was washed with three 50 ml portions of water, and the solvent was evaporated under reduced pressure. Recrystallization of the residue from methanol gave benzyl p-(p-acetoxybenzoyloxy)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04573062
Source datasetuspto-grants-1986_02
ORD IDord-87883dc8031241fd8e3e272d9e36c9c4
Source noteuspto-grants-1986_02